You are invited to a Virtual Bone China Tea Party!

Celebrate National Bone China Tea Day with OI community members!

On Thursday, May 7, OI community members will come together virtually to celebrate National Bone China Tea Day! You are invited to attend the OIF’s virtual Bone China Tea party, hosted by Bone China Tea Chair Susie Wilson. 

THURSDAY, MAY 7, 2020 // 4:00pm ET

Click here to join the Zoom Virtual Meeting

Meeting ID: 879 5237 1329
Password: 049742

 

To set up your own Bone China Tea event or to learn more, visit www.oif.org/campaign/bonechinatea

 

Happy Wishbone Day!

Today is Wishbone Day, the international day of awareness for osteogenesis imperfecta (OI)! Each year on Wishbone Day, OI community members rally together to support and celebrate each other. The OI Foundation will be sharing hourly posts starting at 7:00am ET as part of our annual social media OI awareness campaign. Like, comment, and SHARE to raise OI awareness!

#SHAREforAWARENESS #WishboneDay #UnbreakableSpirit #OIawareness

Raise OI awareness and support the OIF year-round!

Thank you for celebrating #GivingTuesdayNow with the OI Foundation! Remember, you can raise OI awareness and support the OI Foundation year-round!
 
1. Create a Facebook Fundraiser! Visit www.facebook.com/fund/OsteogenesisImperfectaFoundation/ to start one today.
 
2. Host a Bone China Tea! National Bone China Tea Day is this Thursday (5/7). This virtual event is perfect way to connect with loved ones while staying safe at home. Visit www.oif.org/campaign/bonechinatea to get started!
 
3. Plan a virtual Blue Jeans for Better Bones Day! National Blue Jeans for Better Bones Day is this Friday! Invite your friends and family to wear jeans (or a blue shirt) to show support for the OI Foundation. Visit www.oif.org/bjbb to set up your blue jeans day!
 
4. Join the OIF Book Club! Read more, raise more, win more prizes! Visit www.oif.org/campaign/oifbookclub to register today!
 
5. Participate in the virtual Unbreakable Spirit® Walk-n-Wheel on July 10, 2020! Register today as an individual or create a team by going to www.oif.org/campaign/walkandwheel!
 
#GivingTuesdayNow #SHAREforAWARENESS #UnbreakableSpirit

VIRTUAL SPIRIT WEEK Day 1: Read More Monday!

OI Awareness VIRTUAL SPIRIT WEEK Day 1: Read More Monday!

Kick off your week with a good book – join the OIF Book Club!

How it works:
1. Find a sponsor!
Ask your family members and friends to support your reading efforts. You can have as many sponsors as you want!
2. Read books.. raise money!
For every book you read, have your sponsor(s) match it with a donation. The more books you read, the more money you will raise! Share photos of the books you read on social media using #OIFBookClub!
3. Win cool prizes!

Visit www.oif.org/campaign/OIFBookClub to sign up today. #SHAREforAWARENESS #OIawareness

National Osteogenesis Imperfecta (OI) Awareness Week begins tomorrow!

National Osteogenesis Imperfecta (OI) Awareness Week begins tomorrow!

How will YOU raise OI awareness this week?
National OI Awareness Week is scheduled around Wishbone Day (May 6), the international day of OI awareness.
There are so many ways to raise OI awareness during OI Awareness Week and Wishbone Day – check out some ideas below!



Update your Facebook Profile Picture! 

Use your Facebook page to raise OI awareness on social media! Click here to add a National OI Awareness Week frame to your Facebook profile picture!

Raise OI Awareness from home!
This year, we will be celebrating National OI Awareness Week with a Virtual Spirit Week! Check out the flyer below!

Play OI Awareness Bingo!
1. SAVE the OIF Bingo card
2. MARK off as many boxes as you can throughout OI Awareness Week
3. SHARE it on your social media pages using #SHAREforAWARENESS!

Monday, May 4 – READ MORE MONDAY
Have you joined the OIF Book Club yet? Share a photo on social media to share what you are reading this week! Use the #OIFBookClub to share with OI community members!

Tuesday, May 5 – #GivingTuesdayNow
#GivingTuesdayNow is a new global day of giving and unity that will take place on May 5, 2020 as an emergency response to the unprecedented need caused by COVID-19. We hope you will celebrate #GivingTuesdayNow with the OI Foundation by making a donation at www.oif.org/donate, or creating a Facebook Fundraiser to benefit the OI Foundation.

Wednesday, May 6 – WISHBONE DAY (International OI Awareness Day)
We can’t wait to see photos of you wearing your Wishbone Day yellow! Each year on Wishbone Day, the OI Foundation shares facts about OI on social media every hour. Make sure you are following the OI Foundation on Facebook, Twitter, and Instagram so you can help us raise OI awareness worldwide by liking and sharing every #SHAREforAWARENESS post!

Thursday, May 7 – NATIONAL BONE CHINA TEA DAY
Invite your friends and family to join you on video call (try using Skype, Zoom, or Facetime) for a virtual tea party! Choose a dress code for your guests – formal, casual, or pajamas! Start planning your Bone China Tea virtual event at www.oif.org/campaign/bonechinatea/

Friday, May 8 – BLUE JEANS FOR BETTER BONES DAY
Create your Blue Jeans for Better Bones online page and we’ll send you and any donors a special badge to add to your Facebook or Instagram profile. Share your photos with us using the hashtag #OIFphotocontest to be entered into the 5 Decades of Denim photo contest in honor of the OIF’s 50th anniversary. For extra credit, share a #FlashbackFriday photo featuring your stylish jeans over the decade!

For more information, visit www.oif.org/awarenessweek

 

Thank you for proclaiming National OI Awareness Week in your state!
So far, we have received 16 official National OI Awareness Week proclamations! Thank you to the OI community members for who requested proclamations, and to the government officials who proclaimed May 2-9, 2020 as National OI Awareness Week in their state!
Click here to view all National OI Awareness Week 2020 proclamations.

If you have received a proclamation for your state, please send a photo to Christina at cteufert@oif.org

 

Happy National OI Awareness Week!

We can’t wait to celebrate with you!

In Memory of Gemma Geisman

It is with great sadness that the OI Foundation’s Board of Directors and Staff report that Gemma Geisman, founder of the OI Foundation, has passed away.

More than fifty years ago, Redbook magazine published an article written by Gemma Geisman about her 11-year-old son, Mike, who was living with osteogenesis imperfecta. Gemma wrote about the challenges they faced as a family, including the isolation and the frightening lack of information or support for caring for a child with a rare fragile bone condition. Gemma’s words reached families with OI across the nation. Letters started flooding her mailbox and within months, a committed group of parents came together to support each other. In 1970, the OI Foundation was formed.

Gemma, with the help of a small group of parents, made it her mission to bring information and support to families with OI. Gemma was involved in publishing the first issue of the OIF Breakthrough Newsletter, creating the first brochure about OI, establishing the OI support group network, organizing the first OIF National and Regional Conferences, and so much more.

This year is the OI Foundation’s 50th anniversary year. The OI Foundation would not be here today without Gemma’s dream to bring information and support to families with OI.

We owe a very special thank you to Gemma for her dedication to the OI community for more than fifty years. She will be greatly missed.


Gemma Marquis Geisman 85, peacefully passed away on Thursday, April 23, 2020. She was born in Van Buren, Maine on December 7, 1934 and was proud to be number 12 of 13 children born to William and Adele (Castonguay) Marquis.

Gemma married the love of her life Richard “Dick” Geisman on June 27, 1953 at St. Anne’s Catholic Church in Hartford, CT and they shared 54 wonderful years together before his passing on September 30, 2008. Gemma had plans to be a nun after graduation until Dick, a navy sailor, “crashed” a wedding she was attending. It must have been divine intervention as they were truly meant for each other.

Gemma was a loving mother to her four children and in spite of the fact that her second child, Mike, was born with a rare genetic brittle bone disease called Osteogenesis Imperfecta, she and Dick did everything they could to create a normal family life for all.  Their home became the hub of the neighborhood, with wiffle ball games causing a permanent infield in the grass, homemade ice cream being cranked and shared with all, Christmas trees bigger than life, pulling taffy, making fudge, camping and many more activities that have become family traditions. Her children could always count on her to sweep away the boredom of a lazy summer day by writing a script for a summer play with them as the main characters and the neighborhood children as the audience. Gemma was the producer, director, set designer, costume designer, acting coach and marketing genius. Because of her love of reading there were many trips to the local library and piles of books coming home for the children to read.

Gemma was very creative and had a passion, not only for reading, but for writing stories. She is the published author of over 60 articles that have appeared in various magazines such as Redbook, Good Housekeeping, Lady’s Circle, Exceptional Parent, American Legion Magazine, Catholic Digest and many others. Her favorite topic was sharing the joys of growing up in a small town in Northern Maine in a large French-Canadian family in the “House on the Hill”.

Gemma’s writing led her to submit a Young Mother’s Story to Redbook Magazine in 1967 called “My Prison of Dreams” which was the story of how it felt to care for a breakable baby with Osteogenesis Imperfecta. The publication of this story created a flood of mail from all over the country from parents in similar situations and it changed her life forever. Gemma worked together with a few of those parents and the doctors at the Shriners Hospital in Chicago, where Mike spent many days, and the result was the formation of the Osteogenesis Imperfecta Foundation which celebrates its 50th anniversary in 2020. Thousands of children worldwide, born with this rare disease, and their families have been helped over the years because of Gemma.

Some of Gemma’s roles in the OI Foundation included serving as the Foundation’s first Executive Director (1981-1987), serving on the Advisory Council and the Nominating Committee for many years. She also edited Breakthrough (the foundations newsletter) for 14 years, providing information, inspiration, role models and support to a growing readership. Gemma was awarded the Foundation’s highest honor, the Thelma Clack Lifetime Volunteer of the Year Award in 2002. Gemma told the story of raising Mike and the formation of the OI Foundation in her book “From the Seeds of Sadness” which was published in 2009 and can be found on Amazon.

Gemma has impacted the lives of everyone who has known her and she will be greatly missed. She is survived by her children, Cathy Bowen of Goffstown, NH, Cindy Geisman (Jay Williams) of Bastrop, TX, and Richard “Rick” Geisman (Rose) of East Hartford, CT. Gemma has eight grandchildren, Jennifer Bowen, Emily (Bowen) Blossom, Ryan Bowen, Paula (Bowen) Huntley, Sean(Samantha), Trey and Corey Geisman and Gemma “Gem” Williams. She also has seven great-grandchildren, Jacob and Caleb Shepard, Marshall Bracey, Gavin and Corbin Huntley, who lovingly called her triple G (Great Grandma Geisman) and Carson and Camden Geisman. She is also survived by two siblings Peter Marquis (Angie) of Goffstown, NH and Robertine “Bobbie” Dryer (Chuck) of Portsmouth, NH and a brother-in-law Jim Geisman of Horton, MI along with many nieces and nephews who loved her dearly. Gemma is predeceased by her husband Dick and son Mike, her parents and ten siblings.

A Catholic mass and celebration of her life will be held later this year when it is safe once again to come together. Her ashes will be placed next to Dick in the Woodland Cemetery in Van Wert, Ohio. The family requests that in lieu of flowers, donations be made to The Gemma Geisman Funds at the Osteogenesis Imperfecta Foundation, 804 W Diamond Ave Suite 210. Gaithersburg MD 20878 or online at www.oif.org.

Obituary: Gemma Geisman 

 

Pneumonia Vaccine Update

The Foundation is continually developing new information resources in response to the needs of families, individuals, and professionals working with those affected by OI. Thank you to Dr. Robert Sandhaus (University of Colorado School of Medicine, Denver, CO) for helping us update the fact sheet listed below.

Pneumonia Vaccine Update – Information for Children and Adults who have OI

The OI Foundation has published fact sheets on many topics related to understanding and living with OI. View all OIF Fact sheets at www.oif.org/informationcenter/factsheets/.